{
  "id": 23157,
  "label": "radial defect robin sequence",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0043191",
  "properties": {
    "xrefs": [
      "GARD:0004624",
      "MEDGEN:419346",
      "MESH:C536261",
      "UMLS:C2931143"
    ],
    "synonyms": [
      "Bruce Winship syndrome",
      "Bruce winship syndrome",
      "bilateral radial defects club foot deformity micrognathia and cleft palate",
      "bilateral radial defects, club foot deformity, micrognathia and cleft palate"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 11072,
      "label": "isolated Pierre-Robin syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004347",
          "MEDGEN:19310",
          "MESH:D010855",
          "NCIT:C85010",
          "NORD:1579",
          "OMIM:261800",
          "Orphanet:718",
          "SCTID:4602007",
          "UMLS:C0031900",
          "icd11.foundation:136361299"
        ],
        "synonyms": [
          "Pierre Robin Sequence",
          "isolated Pierre Robin sequence",
          "Pierre Robin syndrome skeletal dysplasia polydactyly",
          "glossoptosis, micrognathia, and cleft palate"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Pierre-Robin syndrome (or Pierre-Robin sequence) is characterized by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft."
      },
      "child_count": 1,
      "reference_id": "MONDO:0009869"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 11072,
      "label": "isolated Pierre-Robin syndrome"
    }
  ]
}